Department of Physiology and Pharmacology, Basic Sciences, School of Medicine, Loma Linda University, Loma Linda, CA, USA.
Department of Anesthesiology, Neurosurgery and Neurology, Loma Linda University School of Medicine, Loma Linda, CA, USA.
J Neurosci Res. 2020 Nov;98(11):2275-2289. doi: 10.1002/jnr.24709. Epub 2020 Aug 9.
Role of peroxisome proliferator-activated receptors (PPARs) in the pathophysiology of stroke and protective effects of PPAR ligands have been widely investigated in the last 20 years. Activation of all three PPAR isoforms, but especially PPAR-γ, was documented to limit postischemic injury in the numerous in vivo, as well as in in vitro studies. PPARs have been demonstrated to act on multiple mechanisms and were shown to activate multiple protective pathways related to inflammation, apoptosis, BBB protection, neurogenesis, and oxidative stress. The aim of this review was to summarize two decades of PPAR research in stroke with emphasis on in vivo animal studies. We focus on each PPAR receptor separately and detail their implication in stroke. This review also discusses recent clinical efforts in the field and the epidemiological data with regard to role of PPAR polymorphisms in susceptibility to stroke, and tries to draw conclusions and describe future perspectives.
在过去的 20 年里,过氧化物酶体增殖物激活受体 (PPAR) 在中风的病理生理学中的作用及其配体的保护作用已得到广泛研究。大量的体内和体外研究都证明,所有三种 PPAR 同工型(尤其是 PPAR-γ)的激活均可限制缺血后损伤。PPAR 已被证明作用于多种机制,并被证明可激活与炎症、细胞凋亡、血脑屏障保护、神经发生和氧化应激相关的多种保护途径。本综述的目的是总结过去 20 年中风的 PPAR 研究,重点是体内动物研究。我们分别关注每个 PPAR 受体,并详细说明它们在中风中的作用。本综述还讨论了该领域的最新临床研究以及关于 PPAR 多态性在中风易感性方面的流行病学数据,并试图得出结论和描述未来展望。